Critical function of T cell death-associated gene 8 in glucocorticoid-induced thymocyte apoptosis

Int Immunol. 2003 Jun;15(6):741-9. doi: 10.1093/intimm/dxg070.

Abstract

Transcriptional expression of a gene or genes is absolutely required for induction of glucocorticoid-induced thymocyte apoptosis. We have previously shown that expression of T cell death-associated gene 8 (TDAG8) is quickly induced exclusively in the thymus after dexamethasone (DEX) treatment. Here, we present data that TDAG8 expression is induced prior to induction of DEX-mediated apoptosis. In contrast, TDAG8 expression in thymocytes was not induced in the process of gamma-irradiation-mediated apoptosis. TDAG8 expression accelerated only DEX-induced, but not TCR-mediated or gamma-irradiation-induced, thymocyte apoptosis in transgenic mice overexpressing TDAG8. Interestingly, these effects were specifically detected in CD4(+)CD8(+) double-positive thymocytes. Moreover, activation of caspase-3, -8 and -9 was enhanced in thymocytes of TDAG8 transgenic mice after DEX stimulation. In conclusion, TDAG8 expression is involved in glucocorticoid-induced signals to activate caspase-9, -8 and -3 for subsequent apoptosis induction in CD4(+)CD8(+) double-positive thymocytes.

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Apoptosis / genetics*
  • Apoptosis / radiation effects
  • Blotting, Northern
  • Blotting, Western
  • Caspases / drug effects
  • Caspases / metabolism
  • Cells, Cultured
  • Enzyme Activation / drug effects
  • Female
  • Gene Expression Regulation / drug effects
  • Gene Expression Regulation / immunology*
  • Glucocorticoids / pharmacology*
  • In Situ Nick-End Labeling
  • Mice
  • Mice, Transgenic
  • Receptors, G-Protein-Coupled / genetics*
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / pathology
  • T-Lymphocytes / physiology*

Substances

  • GPR65 protein, mouse
  • Glucocorticoids
  • Receptors, G-Protein-Coupled
  • Caspases